by Ursula Tschorn | Jul 5, 2015
ISO ist the short form of the International Organization for Standardization. It is an international standard-setting body composed of representatives from various national standards organizations. Founded on 23 February 1947, the organization promotes worldwide...
by Ursula Tschorn | Jul 5, 2015
The EMA and the EU Regulatory Network have founded an EU IDMP Task Force with the involvement of terminology organisations, software vendors and developers of medicinal products dictionaries or databases. The task force will be responsible for advising on the...
by Ursula Tschorn | May 24, 2015
Pharmaceutical Product Identification (PhPID)
by Ursula Tschorn | May 22, 2015
HL7 – Health Level Seven Health Level-7 or HL7 refers to a set of international standards for transfer of clinical and administrative data between software applications used by various healthcare providers. These standards focus on the application layer, which...
by Ursula Tschorn | May 22, 2015
Master Data Management (MDM) is critical for IDMP compliance In matching IDMP´s required data with customer´s data there will be several systems identified which hold IDMP relevant data. In case of Marketing Authorisation Holders (MAHs) this will be Regulatory...
